Philips Respironics announced a recall for Continuous and Non-Continuous Ventilators (certain CPAP, BiLevel PAP and Ventilator Devices) due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices. For information on the Medical Device Recall, a complete list of impacted products, and potential health risks, visit philips.com/src-update.

We know that you have questions and concerns.  Please contact our patient care team at [email protected] with your name, email address and telephone number. We will provide updated information from Philips as soon as it becomes available.  As always, your primary health care provider is best positioned to assist with specific health care concerns.